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Human Molecular Genetics 21
Showing records 1 to 21 | Display all abstracts in Human Molecular Genetics98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Cui X
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Guggenheim JA; Clark R
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Kim HJ
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Cui J
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Cheng CH
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Terry L
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Jenny LA; De Carvalho Junior JRL
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Patasova K
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Chang YJ
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Haarman AEG; Musolf AM
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Kong Y; Hsu CW
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Verhoeven VJM
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Huang IW
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Klaver CCW
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Huang IW
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Bailey-Wilson JE
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Ragi SD; Lin CS
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Hysi PG; Williams C
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Li X
Human Molecular Genetics 2022; 31: 2438-2451
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Human Molecular Genetics 2022; 31: 1909-1919
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Sparrow JR; Tsang SH
Human Molecular Genetics 2022; 31: 2438-2451